Home NDC 12634-697 acyclovir
Product NDC 12634-697
11-digit product format 126340697
Labeler code 12634
Product ID 12634-697_271bf420-cc51-52eb-e054-00144ff8d46c
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form TABLET
Route ORAL
Labeler Apotheca Inc.
Application ANDA077309
Marketing category ANDA
Marketing start 2006-03-13
Marketing end 0000-00-00
Substance ACYCLOVIR
Active strength 800 mg/1
Pharmacologic classes DNA Polymerase Inhibitors [MoA],Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [EXT]
NDC exclude flag No
Listing certified through 2019-12-31
Current FDA listing Historical FDA.report record DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 12634-697 ACYCLOVIR TABLET [APOTHECA INC.] 4 Legacy NDC, 10 package rows 20151218_271bfbb6-4990-500a-e054-00144ff8d46c.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Status 12634-697-01 12634069701 100 in 1 BOTTLE Historical 12634-697-09 12634069709 35 in 1 BOTTLE Historical 12634-697-54 12634069754 14 in 1 BLISTER PACK Historical 12634-697-55 12634069755 15 in 1 BLISTER PACK Historical 12634-697-61 12634069761 10 in 1 BLISTER PACK Historical 12634-697-65 12634069765 5 in 1 BLISTER PACK Historical 12634-697-71 12634069771 30 in 1 BOTTLE Historical 12634-697-79 12634069779 25 in 1 BOTTLE Historical 12634-697-90 12634069790 90 in 1 BOTTLE Historical 12634-697-91 12634069791 1 in 1 BLISTER PACK Historical